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I am Living with a Diagnosis of Myelofibrosis

I was diagnosed with myelofibrosis on October 5, 2018, at the Cleveland Clinic. I’m still trying to figure it out as I had never heard of it before. I was having blood draws every week but have now increased to every 2 weeks. I’m tracking that as I was never a medical person and everything is new. Also joined an MF support group which has been very helpful!

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Comments

  • Anthony Carrone moderator
    6 months ago

    Hey, @Sandy 🙂 How are you doing today? Just wanted to stop by and say I was thinking about you and hoping you’re still finding your support groups helpful. Hope you are staying warm during this arctic blast! Warmly, Anthony

  • Ann Harper moderator
    6 months ago

    Good luck to you. Please keep us informed about your progress.

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